Manufacture of a reinforced, non-woven textile fiber sheet material

ABSTRACT

This invention relates to a random fiber sheet material having regions in which fiber cross-over points are bonded by synthetic elastomer binder, the regions being separated within the material by regions in which there is no bonding of fiber cross-over points. The invention also relates to a process for the preparation of the material.

States atent [1 Hammer et all.

11] 3,853,608 [451 Dec. 10, 11974 MANUFACTURE OF A REINFORCED, NON-WOVEN TEXTILE FIBER SHEET MATERIAL Inventors: Klaus-Dieter Hammer, Mainz;

Ludwig Klenk, Hallgarten, both of Germany Assignee: Kalle Alktiengeseilsehaft,

Wiesbaden-Biebrich, Germany Filed: Sept. 22, 1972 Appl. No.: 291,323

Foreign Application Priority Data Septv 24, 1971 Germany 2147757 US. Cl. 117/140, 117/76 F, 156/329, 156/331,161/157,161/170,161/206, 161/D1G. 2, 260/292 Int. Cl. C08c 17/16 Field of Search 156/622, 327, 329, 331; 161/157, 169, 170, 176; 117/140, 76F

Primary Examiner-George F. Lesmes Assistant Examiner-James J. Bell Attorney, Agent, or FirmJames E. Bryan [5 7] ABSTRACT This invention relates to a random fiber sheet material having regions in which fiber cross-over points are bonded by synthetic elastomer binder, the regions being separated within the material by regions in which there is no bonding of fiber cross-over points. The invention also relates to a process for the preparation of the material.

9 Claims, No Drawings MANUFACTURE OF A REINFORCED, NON-WOVEN TEXTILE FIBER SHEET MATERIAL This invention concerns a process for the manufacture of a nonwoven textile fiber sheet material bonded by chemical means, which has a high tensile strength and tear propagation strength and an s-shaped course of its stress-strain diagram with a low initial modulus. Fleeces having these physical properties are particularly suitable for use as substrates for the manufacture of leather-like material for garment purposes, of material for the manufacture of handbags and the like, and for technical uses.

It is known to incorporate synthetic polymers into fiber fleeces and to reinforce the latter thereby. For this purpose, the fleeces are impregnated with solutions or dispersions of suitable elastomers and the polymer is then deposited in the fleece by coagulation. In the course thereof, the elastomer is preferentially absorded at the cross-over points of the fibers and deposits in compact layers on the walls of the cavities of the fleece.

The known processes for bonding fleeces have the disadvantage that it is not possible reliably to avoid excessive bonding" or inadequate bonding" in the whole of the fleece or parts thereof. The known processes therefore give only fiber fleeces which are not entirely satisfactory as regards their mechanical properties. The stress-strain curve of the fleeces bonded in accordance with the known processes shows a positive curvature. It immediately rises rapidly, and a low initial modulus of such fleeces is not achievable by known processes. This fact is of particular disadvantage if these fleeces are further converted into leather-like material, from which, for example, shoe uppers are manufactured.

The tear propagation strength and resistance to pulling out of stitches, and the rolling and creasing behavior of fleeces manufactured according to known processes is unsatisfactory; the fleeces are hard and crinkly.

The present invention provides a process for the manufacture ofa chemically bonded non-woven textile fiber sheet material, wherein a. a non-woven textile fiber sheet material is treated with a binder liquid composed of an aqueous dispersion of a synthetic elastomer containing chemically reactive groups and a solution of silicone oil in toluene,

b. theinaterial is freed from excess of binder liquid,

c. the resulting material is subjected to the action of heat,

d. the resulting material is treated with an impregnating liquid as herein defined,

e. the material is freed from excess of impregnating liquid.

f; the resulting material is subjected to the action of heat,

g. the resulting material is treated with a liquid containing a synthetic elastomer,

h. the material is freed from excess of elastomer liquid,

i. the elastomer is deposited by coagulation in the cavities in the material, and

j. the resulting material is subjected to the action of heat for drying or drying and crosslinking of the deposited elastomer.

The resulting bonded fleece does not display the disadvantages of the known fleeces so that it is neither excessively bonded nor inadequately bonded and pos- I sesses an S-shaped course of the stress-strain curve, with low initial modulus, high tensile strength and tear propagation strength and displays the leather-like properties which are closely associated with these physical properties.

The bonded fiber fleece of the invention is such that the binder is spatially distributed therein at centers of bonding in the form of segregated regions and the parts of the fleece lying between these regions are unbonded.

The invention accordingly, further provides a random fiber sheet material having regions in which fiber cross-over points are bonded by synthetic elastomer binder, the regions being separated within the material by regions in which there is no bonding of fiber crossover points.

In the first series of process steps, the fleece is bonded by subjecting it to the action of a binder liquid which is composed of an aqueous dispersion of a synthetic elastomer containing reactive groups and a solution of Silicone oil in toluene.

The reactive groups of the elastomeric binder enable the latter to react, under the action of heat and, advantageously, with the conjoint use of crosslinking catalysts, with chemical compounds which possess reactive groups, so as to undergo crosslinking.

The aqueous dispersion used for the manufacture of the binder liquid may have a polymeric solids content in the range of 5 to 30% by weight, preferably in the range of 10 to 20% by weight, relative to the total weight of the dispersion. The solution of silicone oil in toluene may contain 10 to 50% by weight of silicone oil relative to the total weight of this solution.

The binder liquid is manufactured by mixing the two above-mentioned liquids with one another. The solution of silicone oil in toluene may be added to the clastomeric dispersion in an amount in the range of 8 to 60 g, preferably 20 to 40 g, per liter of dispersion.

The dispersed phase of the aqueous dispersion is composed of a synthetic elastomer with reactive groups, especially COOH /orCON(CH OI-I) groups.

Synthetic elastomers based on acrylic copolymers are preferred, especially acrylic copolymers which are composed of 3 or 4 chemically different acrylic compounds. At the same time it is essential that the copolymers should be composed to the extent of at least 5% and at most 25% of acrylic compounds with free reactive groups. Butyl acrylate is preferred as quantitatively the main constituent of the copolymers.

Mixtures of copolymers of the specified type also can be used in the dispersed form.

A particularly preferred aqueous copolymer dispersion consists of approximately 92% by weight of butyl acrylate, approximately 4% by weight of methacrylic acid and approximately 4% by weight of acrylamide. The dispersion has a solids content of 40% by weight relative to the total weight of the dispersion.

Another preferred aqueous copolymer dispersion consists of approximately 86% by weight of butyl acrylate, approximately 4% by weight of itaconic acid, ap-

and/or CONH and-' proximately 8% by weight of dimethylolmethacrylamide and approximately 2% by weight of methacrylic acid. The solids content of the dispersion is 42% by weight.

Apart from the synthetic elastomers based on polyacrylate which have been stated to be preferred and which function as fiber binders, it is possible to use polyurethanes or synthetic rubbers, provided that they still contain reactive groups, for example polyurethanes with free OH and/or COOH groups and/or polyurethanes which still possess reactive isocyanate groups. An example of an elastomer suitable for fiber bonding is a copolymer based on butadiene-acrylonitrilemethacrylic acid. I I

In the first process step, the binder liquid is allowed to act on the fiber sheet, for example by impregnating the sheet in the liquid. The impregnated fleece is thereafter freed from excess binder liquid by squeezing out, for example .in the nip of a pair of rollers.

The impregnating liquid which acts on the fleece in the fourth process step contains one or more synthetic coating agents. By synthetic coating agents there are to be'understood chemical compounds which are capable of forming acoating on the fiber surface which after the action of sufficient heat on the fibers coated with the agent is firmly bonded to the'fiber surface as a result of the high adhesion between the fiber surface and coating caused by the action of heat.

Suitable coating agents are: ethylene ureas of the general formula ll CH wherein R is an aliphatic chain with 14 to 22 carbon atoms, fatty'amines having a carbon chain of 16 to 18 carbon atoms, paraffins, etherified fat-modified synthetic resins with side chains of between l2 and 18 carbon atoms, cross-linkable an'd non-cross-linkable silicones, such as, for example, dimethyl-polysiloxane and hydrogenomethyl-polysiloxane or cross-linkable polymers suitable for'textile finishing, which possess perfluorinated aliphatic side chains (for example, Scotchgard" Registered Trade Mark of Minnesota Minning and Manufacturing Co., U.S.H.). Suitable crosslinkable polymers have a perfluorinated aliphatic side chain with 6 to 14, especially 8 to 12, carbon atoms.

For example, in a cross-linkable polymer containing carboxyl groups the perfluorinated cross-linkable aliphatic side chains can be bonded to the carboxyl group of the polymer by a sulfonamide group.

The coating agent must possess the inherent properties that no, or virtually no, physical bonding forces act between adjacent surfaces of the coating and surfaces of the consolidating material, i.e., the adhesion between the surfaces is so slight that only sliding displacement of the surface relative to one another is possible under the action of external mechanical force on the fleece, for example on bending or stretching the fleece.

The coating agent is introduced into the fleece in the form of a liquid solution or dispersion the impregnating liquid by, for example, impregnating the fleece with the liquid and then expelling the solvent or dispersing agent, for example by the action of sufficient heat on the fleece, A liquor ratio in the range of 1:10

to 1:50, especially of l:l0 to 1:30, is preferred. Suitable liquids for the manufacture of a solution which contains the coating agent are those which do not have a solvent action on the fibers of the fleece, for example water.

Suitable dispersing agents for the manaufacture of a liquid dispersion of a coating agent are those which do not have a solvent action on the fibers of the fleece, for example water.

The proportion of coating agent in the impregnating liquid may be in the range of 2 to 30% by weight relative to the total weight of the impregnating liquid, and especially in the range of 6 to 12% by weight.

The coating agent is to be regarded as bonded in a wash-resistant manner to the fiber surface if the adhesion between the fiber surface and the coating agent is so great that on five mechanical washes at C. according to DIN 54,010 no detachment, or virtually no detachment, of the coating agent from the fiber surface occurs.

A suitable wash liquid is: 5 g/l of soap and 2 g/l of anhydrous sodium carbonate, washing time 30 minutes, 60C., i250 liquor ratio.

The elastomer liquid incorporated into the fleece in the seventh process step is composed of a solution of a synthetic elastomer in an organic solvent or of an aqueous dispersion of a synthetic elastomer.

Aqueous elastomer dispersions are preferred. A suitable elastomer solution is, for example, polyurethane in dimethylformamide. An aqueous dispersion of a copolymer based on butadiene-acrylonitrile-methacrylic acid is preferred and copolymers containing approximately 64% by weight of butadiene approximately 32% by weight of acrylonitrile and approximately 4% by weight of methacrylic acid, in each case relative to the total weight of the copolymer, are very particularly preferred.

The proportion of elastomer in the solution may be 20 to 40% by weight, relative to the total weight of the solution. The proportion of polymer in the elastomer dispersion may be 20 to 50% by weight, relative to the total weight of the dispersion.

Suitable non-woven textile fiber sheets are those which consist wholly or predominantly of synthetic fibers; the snythetic fiber content of the fleece can consist either of fibers which are chemically of the same nature or of a mixture of fibers of different chemical composition; for example, a random fiber fleece can be made up of 50% of polyester and 50% of polyamide fibers.

The fleece density may be in the range of 0.08 to 0.6 g/cm Mechanical pre-consolidation and densification of the raw fleece is possible by needle-punching or by needle-punching and shrinkage, if heat-shrinkable fibers are used in the fleece. Fleece densities of between 0.3 and 0.6 g/cm can only be brought about by subsequent calendering of the fleece at elevated temperatures.

In the case of fleeces which are used as substrates for the manufacture of leather substitutes or for textile uses, it is advisable conjointly to use a proportion (up to 50 to 60%) of natural fibers (cellulose or wool) or hydrophilic fibers, such as reclaimed fibers or polyvinyl alcohol fibers, in order in this way to achieve favorable physiological properties.

The original fleeces have a very flat shape of the stress-strain curve, with a low initial modulus, The course of the curve namely initial modulus, middle section and destruction phase can be varied within wide limits in the original fleece through the nature of the fibers chosen, their titre, the fiber orientation, the length and surface characteristics of the fibers and the density of the fleece.

In order to achieve an S-shaped course of the stressstrain curve, and high tensile strength and tear propagation strength values by chemical bonding of the fleece it is necessary to use binder liquids which have a relatively low content of fiber-binding elastomers. It

is an essential condition of the process according to the invention that the aqueous binder dispersion should contain a synthetic elastomer which can be coagulated by heat.

Particularly advantageously, the binder liquid contains a chemical compound which makes it possible for the elastomer to coagulate spontaneously under the action of sufficient heat. Suitable agents which influence the ease of coagulation of the elastomer by heat are, for example, polysiloxanes.

The proportion of the fiber-bonding elastomer in the fleece according to the invention may be in the range of 5 to 30% by weight relative to the starting weight of the original fleece.

The action of heat on the fleece, after the latter has been treated with the binder liquid, first results in the removal of the dispersing agent and, second, in the cross-linking of the elastomer by chemical reaction via its reactive groups.

The consequence of the action of the impregnating liquid, with subsequent heat treatment of the impregnated fleece,'is that on the surface of the parts of the fibers which are free from elastomeric binder, a firmly adhering coating is formed which on subsequent incorporation of elastomer into the fleece prevents the polymer of the elastomer from adhering to the fiber surfaces and to the binder; accordingly, the polymer introduced into the fleece after the impregnating process does not contribute to the bonding of the fibers but exists in the form of globular particles in the cavities of the fleece, without being bonded to the adjoining fiber surfaces.

In the fleece according to the invention, the synthetic elastomer which binds the fibers is localized in the form of a plurality of segregated regions arranged spatially relatively remote from one another in the fleece, within which regions the fibers and fiber cross-over points enclosed by the elastomer are bonded by the chemical binder while the fiber regions and fiber cross-over points located between the segrated binder regions are not bonded.

In contrast to known chemically bonded fleeces in which the chemical binder isv distributed normally at random in the fleece, the fleece according to the invention is distinguished by segregated regions of binder; the overall structure of the binder in the fleece can be described as honeycomb-like.

The result of the first series of process steps is that the desired distribution of the chemical binder in the fleece is achieved. The coagulation conditions of the elastomeric binder should be so chosen that spontaneous coagulation occurs only after the elastomer dispersion has spread horizontally in the fleece and before migration of the dispersion at right angles to the horizontal plane commences. The appropriate coagulation conditions can be determined by simple preliminary experiments in each individual case.

During the course of the first series of process steps, the desired distribution of the chemical binder in the fleece is achieved. As a result of the deposition of the chemical binder in the form of a plurality of spaced regions within the fleece and as a result of cross-linking of the chemical hinder, the fleece becomes reinforced only within the stated regions by relatively large binder particles. When arranged in this way in the fleece, the chemical binder is very much more effective than in the case of diffuse distribution, with small binder particles distributed essentially at random over the cross-section of the fleece. The highest bonding strength is achieved when the adhesion of the binder to the fibers and the cohesion of the binder differ as little as possible from the fiber strength.

The concentration and the amount of the silicone oil solution in aromatic solvents, and the coagulation conditions for precipitating the elastomeric binder from the binder liquid must be suited to the particular binder concentration in the binder liquid and to the binder type. The above-mentioned conditions must at the same time be so chosen that the particular binder concentration gives an optimum as regards mesh width," i.e., as regards the spacing of the individual regions containing binder. lt easily can be: seen that for an in,- creasing binder concentration (increasing binder content of the fleece) the mesh width" of the bonded fiber cross-over points in the fleece must decrease.

Thus if the fleece density remains the same and the type of binder remains the. same, harder types of fleece, with a steep course of the stress-strain curve, increasing tensile strength and decreasing tear propagation strength are obtained as the binder concentration increases.

The mechanical properties of the fleece as a result already can be determined after the preliminary bonding according to the process steps (a) to (c).

In particular, it is advantageous to select the use of a suitable combination of fleece density and optimum binder concentration. For each fleece density, only a very particular binder concentration (a very particular binder content) can be used to give effectively the optimum mesh width.

The development of the honeycomb structure of the binder in the fleece can be intensified by increasing the concentration of the silicone oil solution in the aromatic solvent, which is added to the elastomer dispersion or elastomer solution.

Depending on the density of the fleece, the proportion of the synthetic elastomer embedded in the fleece and not contributing to fiber bonding is 10 to 50% by weight relative to the bonded and impregnated fleece.

A random fiber sheet based on synthetic fibers is impregnated with binder liquid and is thereafter freed from excess of binder liquid, for example by expressing the fleece web in the nip of a pair of rollers. Thereafter,

the fleece is sufficiently heated at a temperature of 120 to 180 C for'a period in the range of 30 seconds to 30 minutes to initiate the coagulation and expel the liquid volatile constituent of the binder liquid, and to cross-link the elastomeric binder.

Thereafter, the bonded fleece is subjected to the action of an impregnating liquid, for example by immersing the fleece in this liquid. The impregnated fleece is then freed from excess of impregnating liquid, for example by expressing in the nip of a pair of rollers. The impregnated fleece is then heated at a temperature in the range of 100 to 170 C for a period in the range of 30 seconds to minutes, as a result of which the fleece is dried and the impregnating agent is crosslinked to give a coating which adheres firmly to the surface of the fiber which are free from elastomeric binder and on the binder.

Thereafter, synthetic elastomer is embedded in the cavities of the impregnated fleece, without adhering to the fibers, by treating the fleece with a polymer solution or polymer dispersion, for example by impregnating the fleece therewith, freeing the fleece from excess of polymer liquid, for example by expressing the fleece in the nip of a pair of rollers, and subjecting the fleece to sufficient heat to cause the precipitation of the clastomer in the form of globular particles in the cavities of the fleece. The coagulation temperature is roughly in the region of 40 C.

After the elastomer hasbeen coagulated, the liquid still contained in the fleece is expelled, for example by drying the fleece in a tenter frame drier at a temperature which suffices to expel the volatile constituents, for example 100 to 120 C. The fleece is then subjected to a temperature in the range of 120 to 180 C i briefly indicated:

In the original fleece, the composition, orientation, length and titre of the fibers and the density of the .fleece can be varied. Furthermore, the type, amount and mesh width of the binder, the substance used as the finish and the amount applied, and also the amount and type of the filler, can be chosen as desired. In the case of the filler, prime factors are the plastic-elastic and the physiological-hygenie properties.

The complicated structure of the material necessary to produce the required mechanical properties can be achieved by verys'imple process steps. The properties concerned are the following mechanical leather-like properties:

The most important characteristic is an S-shaped course of the stress-strain curve, with a low initial modulus. This curve can be adjusted as desired. It is an important pre-requisite that the starting fleece should be isotropic over its surface. Such a characteristic shape of the curve cannot be achieved by any of the previous methods of bonding. The important property ofsuppleness depends on thi's course of the curve. A material can be described as supple if, when stressed mechanically it can easily. give to a slight stress- (flat initial course and low initial modulus) while it offers increasing resistance to a greater stress (steep middle part of the curve). A steep initial course of the curve, i.e., a positive curvature, was hitherto the decisive disadvantage of all synthetic leathers and the reason why shoes made of this material did not wear in." All other mechanical leather-like properties are closely related to the S-shaped course of the curve: a high tear propagation strength is achievable because the force which is applied is transferred to the consolidated fiber network and is reduced by a slight deformation of this network. The tensile strength is very high because the closely delineated bonded regions are very strong. A permanent surface stretching now also becomes possible, and this depends on the filler content. The stretching can be matched to the type ofleather that it is desired to simu late. The rolling and creasing behavior is very leatherlike since the reinforced fiber network and the filler can move independently of one another. As a result of this double bonding process, the differences in density of the fleece are also completely compensated since the binder is drawn into the regions where there is a high density of fibers while the filler is repelled, by the finish, into the regions where there is a low fiber density. It can be appreciated that both a leather substitute and a textile material can be obtained, as desired, by simple measures, and that these materials have hitherto unattainable mechanical properties.

The following Examples futher' illustrate the invention:

EXAMPLE 1 A random fiber fleece of 50% of polyester fibers and 50% of polyamide fibers staple length 30 mm, titre 1.3 dtex which has a density of 0.15 g/cm, a tensile strength of0.4 kp/mm (DlN 53,328) and a tear propagation strength of 8.5 kp/mm (according to [UP 8) is impregnated with a binder liquid of the following composition:

500 g of a 40% by weight aqueous dispersion of a copolymer of the following composition:

92% by weight of butyl acrylate, 4% by weight of methacrylic acid, and 4% by weight of acrylamide 500 g of H O 22.4 g of polysiloxane (for example Coagulant WS of Farbenfabriken Bayer), and

33 g of a 15% by weight solution of silicone oil in toluene (for example Silicone Oil AL of Wacker- Chemie) in a trough filled with this liquid, withdrawn from this trough and freed from excess of liquid by squeezing out in the nip of a pair of rollers.

The fleece is than heated at 180 C for a period of 3 minutes, by radiation from an infra-red radiator;

The bonded fleece is then impregnated in an impreg nating bath containing g of dimethylpolysiloxane (for example Primenit" SW of Farbwerke Hoechst AG) per liter of liquor. The fleece is impregnated with the impregnating liquor or a Foulard machine.

After removing the impregnated fleece from the impregnating liquor, the excess of impregnating liquid is expressed from the fleece in the nip of a pair of rollers and the fleece is then dried in a tenter frame drier at 100 to C and subsequently heated in this drier at C. for a period of 30 seconds.

The impregnated fleece is then dipped in an aqueous dispersion of a copolymer consisting of 64% by weight of butadiene, 32% by weight of acrylonitrile and 4% by weight of methacrylic acid (for example Perbunan NT of Farbenfabriken Bayer), withdrawn from the impregnating bath and then freed from excess of dispersion by expressing in the nip of a pair of rollers. The elastomer is then coagulated on the fleece by heat from an infra-red radiator. The coagulation temperature is 30 C.

Thereafter, the fleece is dried in a tenter frame drier at 100 C and is then heated at a temperature of 160 C for 5 minutes. This heat treatment vulcanizes and cross-links the elastomer.

The fleece is soft and supple and can be used as a substrate for the manufacture of a synthetic material having properties resembling box calf. The fleece has the following characteristics:

Total elastomer content 45% by weight relative to the total weight of the fleece Tensile strength 1.4 kp/mm" Tear propagation strength 12 kp/mm Force required for 5% 0.05 kp/mm'-'. clonagation EXAMPLE 2 As Example 1, except that instead of the aqueous copolymer dispersion mentioned in Example 1, a copolymer dispersion of the composition shown below is employed as constituent of the binder liquid:

500 g of a 40% by weight aqueous copolymer dispersion of the following composition:

86% by weight of butyl acrylate, 4% by weight of itaconic acid,8% by weight of dimethylolmethyacrylic acid amide and 2% by weight of methacrylic acid.

EXAMPLE 3 A random fiber fleece according to Example 1, of density 0.18 g/cm, is treated with a binder liquid of the following composition:

400 g of a 40% by weight copolymer dispersion ofthe following composition:

92% by weight of butyl acrylate, 4% by weight of methacrylic acid, and 4% by weight of acrylamide 600 g of H 0 28 g of polysiloxane (for example Coagulant WS of Farbenfabriken Bayer) and 28 g of a 15% by weight solution of silicone oil in toluene (for example Silicone Oil AL of Wacker- Chemie) by immersion in a bath consisting of this liquid. the further steps leading to fiber bonding being as is Example 1.

The impregnating step is carried out as described in Example 1, except that the impregnating liquid is an aqueous liquid which contains 80 g/l of cross-linkable silicone (for example Akophob" SN of Farbwerke Hoechst AG).

The impregnated fleece is further treated as indicated in Example 1 and there is incorporated an aqueous elastomer dispersion of the following composition:

100 g of a copolymer consisting of 64% by weight of butadiene, 32 by weight of acrylonitrile and 4% by weight of methacrylic acid (for example Perbunan NT of Farbenfabriken Bayer) 1.5 g of an emulsifier (for example Emulvin, 26%

concentration, of Farbenfabrilcen Bayer) 16.5 g of H 0 0.1 g of colloidal sulfur 7.15 g of 32% concentration ZnO 0.1 g of vulcanizing agent Vulkazit" LDA, a product of Farbenfabriken Bayer 0.75 g of vulcanizing agent Vu1kazit" ZU also a product of Farbenfabriken Bayer 2.5 g of titanium dioxide 0.6 g of an emulsifier (for example Emulvin," 40% concentration, of Farbenfabriken Bayer) 29.1 g of octadecyl-ethylene area (for example Primenit" LD of Farbwerke Hoechst AG) 25 g of polyvinyl alcohol (for example *Mowiol N 88 of Farbwerke Hoechst AG) g of H 0 1.65 g of an emulsifier 0.4 g of polysiloxane (for example Coagulant WS) 0.54 g of dyestuff and 0.75 of sodium chloride.

When the fleece has been impregnated in this liquid, it is withdrawn and the excess of liquid is expressed in the nip of a pair of rollers. The fleece is then subjected to the radiation of an infrared radiator and the elasto' mer in the fleece is thereby coagulated (coagulation temperature 38 C). Thereafter the fleece is dried in a tenter frame drier and is then heat-treated for 5 minutes at C, whereby the elastomer is cross-linked.

The fleece produced can be used as a substrate for a synthetic leather substitute having properties resembling soft cowhide.

The fleece has a total elastomer content of 48% by weight relative to the total weight of the fleece, a tensile strength of 1.6 kp/mm a tear propagation strength of 10 kp/mm and a force required for 5% elongation of 0.06 kp/mm". 5

EXAMPLE 4 A random fiber fleece of the composition described in Example 1, having a density of 0.28 glcm, is bonded in the manner described in Example 1 except that the binder dispersion has the following composition:

500 g ofa 40% by weight aqueous dispersion ofa copolymer of the following composition: 92% by weight of butyl acrylate, 4% by weight of methacrylic acid and 4% by weight of acrylamide 800 g of H 0 18.4 g of polysiloxane (for example Coagulant WS of Farbenfabriken Bayer) and 16 g of a 15% by weight solution of silicone oil in toluene (for example Silicone Oil AL of Wacker- Chemie).

The impregnating step is carried out as in Example 2,

using an aqueous liquor of the following composition:

40 g/l of melamine-formaldehyde precondensate (for example Cassurit" MLP of Farbwerke Cassella, Frankfurt/M., Mainkur) 5 g/l of MgCl 12 g/l of a synthetic perfluorinated compound (for example Oleophobol" FC 218 of Chemische Fabrik Pfersee).

Total elastomer content 30% by weight relative to the total weight of the fleece Tensile strength 1.9 kp/nim Tear propagation strength 14 kp/rnm" Force required for 0.08 kp/nnn" elongation EXAMPLE 5 As described in Example 1 except that the random fiber fleece has a density of 0.2 g/cm" and the binder liquid has the followingcomposition:

24.25 g of a 40% by weight aqueous dispersion of a copolymer of the following composition:

92% by weight of butyl acrylate, 4% by weight of methacrylic acid, 4% by weight of acrylamide 7275 g of H 0 1.0 g of magnesium chloride 2.0 g of melamineformaldehyde precondensate,

50% by weight aqueous solution 2.4 g ofa 20% by weight solution of silicone oil in toluene (for example Silicone Oil AL of Wacker- Chemie), and g 2.4 g of polysiloxane (for example Coagulant WS of Farbenfabriken Bayer).

The impregnation of the fleece and the incorportion of the elastomer into the cavities of the fleece are carried out in the manner described in Example l.

.The fleece produced is suitable for use as a substrate for the manufacture of a synthetic material having leather-like properties of the type of soft cowhide.

35% by weight relative to the total weight of the fleece Total elastomer content As described in Example 1, except that the random fiber fleece has a density of 0.14 g/cm" and the binder liquid has the following composition:

360 g of a 40% by weight aqueous dispersion of a copolymer of the following composition:

92% by weight of butyl acrylate. 4% by weight of methacrylic acid, and 4% by weight of acrylamide 540 g of H 0 20 g of magnesium chloride 80 g of a melamine-f0rmaldehyde precondensate,

50% by weight solution 23 g ofa 12% by weight solution ofsiliconc oil in toluene (for example Silicone Oil of Waeker- Chemie), and

23 g of polysiloxane (for example Coagulant WS of Farbenfabriken Bayer).

The impregnation of the fleece and the incorporation of the elastomer into the cavities of the fleece are carried out in the manner indicated in Example 1.

Total elastomer content 42% by weight relative to the total weight of the fleece 1.4 kp/mm 10 kp/mm 0.03 kp/mm' Tensile strength Tear propagation strength Force required for 5% elongation ties is obtained, which can be employed in clothing production.

EXAMPLE 7 A polyester spun fleece of density 0.54 g/cm (filament titre 8 dtex) is bonded in the manner described in Example 1, with binder liquid of the following composition:

360 g ofa 40% by weight aqueous dispersion of a copolymer of the following structure:

92% by weight of butyl acrylate, 4% by weight of methacrylic acid, and 4% by weight of acrylamide 540 g of H 0 g of melamine-formaldehyde precondensate 20 g of magnesium chloride 23 g ofa 15% by weight solution of silicone oil in toluene, and

23 g of polysiloxane.

The fleece is impregnated in the manner indicated in Example 1.

However, in contrast to Example 1, no elastomer is incorporated into the bonded and impregnated fleece. The fleece is split into individual layers parallel to the plane of the fleece. The layers have a weight per unit area of approximately g/m The tensile strength of such a layer is 1.4 kp/mm and the tear propagation strength is 9 kp/mm.

It will be obvious to those skilled in the art that many modifications may be made within the scope of the present invention without departing from the spirit thereof, and the invention includes all such modifications.

What is claimed is:

l. A process for the manufacture of chemically bonded non-woven textile fiber sheet material which comprises a. treating a non-woven textile fiber sheet material with a binder liquid composed of an aqeous dispersion of a synthetic elastomer containing chemically reactive groups and a solution of silicone oil in toluene,

b. eliminating excessive binder liquid from the material,

c. subjecting the resulting material to heat,

d. treating the resulting material with an impregnating liquid,

e. eliminating excess impregnating liquid from the material,

f. heating the material resulting from step (e),

g. treating the resulting material with a liquid containing a synthetic elastomer,

h. eliminating excessive elastomer liquid from the material,

i. coagulating elastomer remaining in the material;

and

j. heating the resulting material.

2. A process as claimed in claim 1, wherein the binder liquid of step (a) contains as said aqueous dispersion an aqueous dispersionn of a copolymer of 92 by weight of butyl acrylate, 4% by weight of methacrylic acid and 4% by weight of acrylamide.

3. A process as claimed in claim 1 wherein the binder liquid of step (21) contains said aqueous dispersion an aqueous dispersion of a copolymer of 8671 by weight of butyl acrylate. 4% by weight of itaconic acid. 871 by weight of dimethylolmethacrylic acid amide and 2% by weight of methacrylic acid.

4. A process as claimed in claim 1 wherein as the elastomer of step (g) there is used a copolymer based on butadiene-acrylonitrile-methacrylic acid.

5. A process as claimed in claim 1 wherein as the elastomer of step (g) there is used a copolymer of approximately 64% by weight of butadiene, approximately 32% by weight of acrylonitrile and approximately 4% by weight of methacryllic acid.

6. A process as claimed in claim 2 wherein as the elastomer of step (g) polyurethane is used.

7. A process as claimed in claim 1 wherein the impregnating liquid of step ((1) contains dimethylpolysiloxane.

8. A process as claimed in claim 1 wherein the impregnating liquid of step ((1) contains a melamineformaldehyde precondensate and a synthetic perl'luorinated compound.

9. A chemically bonded non-woven textile fiber sheet material, when made by the process claimed in claim 1. 

1. A PROCESS FOR THE MANUFACTURE OF CHEMICALLY BONDED NON-WOVEN TEXTILE FIBER SHEET MATERIAL WHICH COMPRISES A. TREATING A NON-WOVEN TEXTILE FIBER SHEET MATERIAL WITH A BINDER LIQUID COMPOSED OF AN AQUEOUS DISPERSION OF A SYNTHETIC ELASTOMER CONTAINING CHEMICALLY REACTIVE GROUPS AND A SOLUTION OF SILICONE OIL IN TOLUENE, B. ELIMINATING EXCESSIVE BINDER LIQUID FROM THE MATERIAL, C. SUBJECTING THE RESULTING MATERIAL TO HEAT, D. TREATING THE RESULTING MATERIAL WITH AN IMPREGNATING LIQUID, E. ELIMINATING EXCESS IMPREGNATING LIQUID FROM THE MATERIAL, F. HEATING THE MATERIAL RESULTING FROM STEP (E), G. TREATING THE RESULTING MATERIAL WITH A LIQUID CONTAINING A SYNTHETIC ELASTOMER, H. ELIMINATING EXCESSIVE ELASTOMER LIQUID FROM THE MATERIAL, I. CONGULATING ELASTOMER REMAINING IN THE MATERIAL, AND J. HEATING THE RESULTING MATERIAL.
 2. A process as claimed in claim 1, wherein the binder liquid of step (a) contains as said aqueous dispersion an aqueous dispersionn of a copolymer of 92 % by weight of butyl acrylate, 4% by weight of methacrylic acid and 4% by weight of acrylamide.
 3. A process as claimed in claim 1 wherein the binder liquid of step (a) contains as said aqueous dispersion an aqueous dispersion of a copolymer of 86% by weight of butyl acrylate, 4% by weight of itaconic acid, 8% by weight of dimethylolmethacrylic acid amide and 2% by weight of methacrylic acid.
 4. A process as claimed in claim 1 wherein as the elastomer of step (g) there is used a copolymer based on butadiene-acrylonitrile-methacrylic acid.
 5. A process as claimed in claim 1 wherein as the elastomer of step (g) there is used a copolymer of approximately 64% by weight of butadiene, approximately 32% by weight of acrylonitrile and approximately 4% by weight of methacrylic acid.
 6. A process as claimed in claim 2 wherein as the elastomer of step (g) polyurethane is used.
 7. A process as claimed in claim 1 wherein the impregnating liquid of step (d) contains dimethylpolysiloxane.
 8. A process as claimed in claim 1 wherein the impregnating liquid of step (d) contains a melamine-formaldehyde precondensate and a synthetic perfluorinated compound.
 9. A chemically bonded non-woven textile fiber sheet material, when made by the process claimed in claim
 1. 